Powder: -20°C for 3 years | In solvent: -80°C for 1 year
GX 201 is a selective NaV1.7 inhibitor, IC50 of < 3.2 nM for hNaV1.7.
説明 | GX 201 is a selective NaV1.7 inhibitor, IC50 of < 3.2 nM for hNaV1.7. |
In vivo | GX 201 has a relatively long half-life in mice. GX 201 produces analgesia at a free plasma concentration about 3 times the IC50 for high-affinity channel block. GX 201 inhibits nociceptive responses induced by formalin and inflammatory pain caused by complete Freund’s adjuvant (CFA)[1]. |
別名 | GX-201 |
分子量 | 563 |
分子式 | C25H27ClF4N2O4S |
CAS No. | 1788071-27-1 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMSO: 60 mg/mL (106.6 mM), Sonication is recommended.
You can also refer to dose conversion for different animals. 詳細
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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc.
GX 201 1788071-27-1 Membrane transporter/Ion channel Sodium Channel GX-201 GX201 Inhibitor inhibitor inhibit